Newborn screening compared to clinical identification of biochemical genetic disorders

Susan E. Waisbren, Catherine Y. Read, Mary G. Ampola, Thomas Brewster, Laurie Demmer, Robert M. Greenstein, C. L. Ingham, Mark Korson, Michael E. Msall, Siegfried M. Pueschel,

Journal of Inherited Metabolic Disease · 2002 · 18 citations · 1 references

Concepts

Abstract

A group of 28 patients with inherited metabolic disease (homocystinuria galactosaemia, maple syrup urine disease and biotinidase deficiency) diagnosed by screening were compared with a group of 17 similar patients identified clinically. The rate of hospitalization was similar for the two groups. The patients diagnosed clinically showed a higher incidence of mental retardation and their parents experienced greater stress and found greater difficulty in meeting their child's needs.

References

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